research associate

Trans Ova Genetics

<div><div><div><div>The Research Associate I will play a vital role in advancing our fibroblast and stem cell gene editing production. This hands ‑ on position is ideal for a highly organized, detail ‑ oriented scientist with strong expertise in cell culture and sterile technique. The successful candidate will support the maintenance and gene editing of bovine cell lines, prepare critical reagents, and contribute to the development, optimization, and documentation of protocols that enable our growing commercial pipeline.<br>
</div></div><div></div><div><div>This position reports to the Research Associate III and will be based in Minneapolis/St. Paul metropolitan area (onsite collaboration required) .<br>
</div></div><div></div><div><div><b>RESPONSIBILITIES<br>
</b></div></div><div></div><div><div><b>Experimental Execution &amp; Commercial Pipeline Processing<br>
</b></div></div><div></div><div><ul><li><div>Execute established workflows to evaluate bovine cell lines, perform gene editing, and assess cell viability for cloning in support of the gene ‑ edited animal production pipeline.
</div></li></ul></div><div><ul><li><div>Design and conduct independent, small ‑ scale experiments to optimize existing processes and improve efficiency; share data, insights, and recommendations with the broader laboratory team.<br>
</div></li></ul></div><div></div><div><div><b>Cell Line Maintenance &amp; Culture Operations<br>
</b></div></div><div></div><div><ul><li><div>Carry out routine culture, passaging, and cryopreservation of bovine stem cell and fibroblast cell lines.
</div></li></ul></div><div><ul><li><div>Prepare and quality ‑ check cell culture media, small molecules, and other critical reagents with precision, consistency, and adherence to laboratory standards.<br>
</div></li></ul></div></div><div></div><div><div><div><b>Data Management &amp; Scientific Documentation<br>
</b></div></div><div></div><div><ul><li><div>Accurately capture experimental results and maintain thorough, well ‑ organized laboratory documentation in accordance with internal policies.
</div></li></ul></div><div><ul><li><div>Partner with senior scientists to learn and apply appropriate data analysis techniques to support experimental outcomes and continuous improvement efforts.<br>
</div></li></ul></div><div></div><div><div><b>Team Collaboration &amp; Project Support<br>
</b></div></div><div></div><div><ul><li><div>Collaborate closely with senior scientists and peers, contributing actively to team discussions, problem ‑ solving , and knowledge sharing.
</div></li></ul></div><div><ul><li><div>Support multiple concurrent projects while effectively adapting to shifting priorities in a dynamic research environment.
</div></li></ul></div><div><ul><li><div>Assist with research activities involving live animals (swine) for up to approximately 20% of the role.<br>
</div></li></ul></div><div></div><div><div><b>PROFESSIONAL QUALIFICATIONS AND EXPERIENCE<br>
</b></div></div><div></div><div><ul><li><div>Bachelor&rsquo;s degree (BS/BA) in a life science&ndash;related field with a minimum of one year of relevant laboratory experience; a combined total of four or more years of education and work experience will also be considered.
</div></li></ul></div><div><ul><li><div>Proficiency in biochemistry, protein analytical techniques, and molecular/cell biology including PCR, cloning, and related workflows.
</div></li></ul></div><div><ul><li><div>Working knowledge of gene ‑ editing tools and methodologies.
</div></li></ul></div><div><ul><li><div>Hands ‑ on experience with DNA, RNA, and protein isolation, purification, and quantitative analysis.
</div></li></ul></div><div><ul><li><div>Hands ‑ on experience in mammalian cell culture, including aseptic technique and routine maintenance.
</div></li></ul></div><div><ul><li><div>Experience with cell ‑ sorting technologies and associated sample preparation.
</div></li></ul></div><div><ul><li><div>Competence in preparing laboratory solutions, buffers, and reagents in accordance with established protocols.
</div></li></ul></div></div><div><div><ul><li><div>Demonstrates exceptional documentation and organizational skills with the ability to maintain high accuracy and attention to detail. Maintains complete and precise documentation using an electronic laboratory notebook (ELN).
</div></li></ul></div><div><ul><li><div>Actively promotes a culture of health, safety, and regulatory compliance within the laboratory environment.
</div></li></ul></div><div><ul><li><div>Demonstrates strong collaboration skills in a cross ‑ functional team setting, with clear and effective verbal and written communication.
</div></li></ul></div><div><ul><li><div>Ability to work effectively under supervisory guidance, consistently executing assigned responsibilities, meeting defined objectives, and adhering to performance expectations.
</div></li></ul></div><div><ul><li><div>Strict adherence to established procedures, protocols, and laboratory standards.
</div></li></ul></div><div><ul><li><div>Participates in rotating weekend laboratory coverage as part of the team&rsquo;s shared schedule.<br>
</div></li></ul></div><div></div><div><div><b>PHYSICAL DEMANDS &amp; WORK ENVIRONMENT<br>
</b></div></div><div></div><div><div>While performing the duties of this job, the employee is regularly required to talk or hear. The employee frequently is required to sit, stand, walk, reach with hands or arms, repetitive hand/wrist activities, and lift up to 40 pounds.<br>
</div></div><div></div><div><div>Specific vision abilities required by this job include close vision, distance vision, color vision, peripheral vision, depth perception and ability to adjust to focus.<br>
</div></div><div></div><div><div>This job operates in a professional office environment. This role routinely uses standard office equipment such as computers, phones, copy machines, filing cabinets and fax machines.</div></div></div></div>

Research Associate

Qatar University

<div><p><b>Job Summary</b></p>
<ul><li>This position will participate in ongoing survey research at SESRI
</li></ul><p><b>Key Responsibilities</b></p>
<ul><li>Participating in the development, design, and implementation of national surveys in Qatar and comparative studies in the GCC region
</li><li>Data analysis
</li><li>Presenting results from surveys administered by SESRI at local and international conferences and to public and private sector audiences
</li><li>Co-authoring papers, articles, and research reports that utilize findings from surveys undertaken by SESRI
</li><li>Teaching seminars in collaboration with personnel from SESRI
</li><li>Collaborating on developing new research projects and grant proposals
</li><li>Participating in the intellectual life of the Institute and University
</li><li>Performing all other duties as assigned</li></ul>
Qualifications
<p></p><p><b>Qualifications</b></p>
<p><b>Education and Certifications</b></p>
<ul><li>Recent doctoral degree from a relevant social science or related discipline
</li></ul><p><b>Languages</b></p>
<ul><li>Excellent proficiency in English and/or Arabic (both written and verbal)
</li></ul><p><b>Experience</b></p>
<ul><li>Knowledge and experience in one or more of the following priority research areas: marriage and family, gender studies, social demography, immigration, migration, and survey methodology
</li><li>Experience in collecting and using survey data</li></ul>
Required Documents<br>
<div></div>
<b>Academic:</b>
<div><ul><li>Current Curriculum Vitae with Cover letter.</li></ul>
<ul><li>Teaching,research, and service philosophy.</li></ul>
<ul><li>Three referees&rsquo; contact information (physical and email addresses as well their telephones contact).</li></ul>
<ul><li>Copy of highest earned credential (transcript of highest degree if graduated from an institution where course work was completed.However, if no course work was completed,an copy of certificate letter from the registrar of your highest credential granting institution regarding your highest academic degree).</li></ul>
<ul><li>Any additional documentation that you feel is relevant to your application.</li></ul></div>
Benefits<br>
<div></div>
<b>Academic:</b>
<div><ul><li>A three-year renewable contract.</li></ul>
<ul><li>Salary is commensurate with experience.</li></ul>
<ul><li>Tax-free salary.</li></ul>
<ul><li>Furnished accommodation in accordance with QU HR policies.</li></ul>
<ul><li>Annual air tickets for faculty member and dependents in accordance with QU HR policies.</li></ul>
<ul><li>Educational allowance for candidate's children (eligible candidates only) in accordance with QU HR policies.</li></ul>
<ul><li>Private health care and health insurance in accordance with QU HR policies.</li></ul>
<ul><li>Annual leave in accordance with QU HR policies.</li></ul>
<ul><li>End-of-contract indemnity.</li></ul></div>
How To Apply <b>New Applicant:</b> You need to setup an account with QU Recruitment Online website (https://careers.qu.edu.qa) and complete your personal profile. Once your profile is complete you may use it to apply for an open Position.</div>

Safoora Publication

<p><b>Responsibilities</b>:</p><ul><li>Evaluation of English notes.</li><li>Proof Reading of English Notes.</li><li>As a book manager, assist in writing new books/notes.</li><li>Assist in preparation of &quot;teacher teaching tips&quot;</li><li>Assist in Preparation of entry test notes.</li><li>Co curricular Development that include lesson plans.</li><li>New look book Development</li><li>Enrichment of data bank of admission test software.</li><li>Coordination of paper and time management.</li><li>Administrative responsibilities of research associate.</li><li>Miscellaneous task assigned by head of research section and principal R &amp; D.</li></ul><p><b>Requirement:</b></p><ul><li>5 to 6 Years of Experience as a Research Associate.</li><li>Masters or M.Phil Degree in English.</li><li>Content development, Textbook Analysis, Teaching and Research skills.</li></ul><p>Job Type: Full-time</p><p>Work Location: In person</p>

Research Associate (English)

<p><b>Responsibilities</b>:</p><ul><li>Evaluation of Chemistry notes</li><li>Proof Reading of Chemistry Notes</li><li>As a book manager, assist in writing new books/notes.</li><li>Assist in preparation of &quot;teacher teaching tips&quot;</li><li>Assist in Preparation of entry test notes.</li><li>Co curricular Development that include lesson plans.</li><li>New look book Development</li><li>Enrichment of data bank of admission test software.</li><li>Coordination of paper and time management.</li><li>Administrative responsibilities of research associate.</li><li>Miscellaneous task assigned by head of research section and principal R &amp; D.</li></ul><p><b>Requirement:</b></p><ul><li>3 to 5 Years of Experience as a Research Associate.</li><li>Masters or M.Phil Degree in Chemistry.</li><li>Content development, Textbook Analysis, Teaching and Research Skills.</li></ul><p>Job Type: Full-time</p><p>Job Type: Full-time</p><p>Work Location: In person</p>

Research Associate (Chemistry)

ICON plc

<div>CRA II- Adverum East coast<p></p><p>
ICON plc is a world-leading healthcare intelligence and clinical research organization. We&rsquo;re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development</p><p></p><p>
Job Advert Posting</p><p>
We are currently seeking a Clinical Research Associate to join our diverse and dynamic team. As a Clinical Research Associate at ICON, you will play a pivotal role in designing and analyzing clinical trials, interpreting complex medical data, and contributing to the advancement of innovative treatments and therapies.</p><p></p><p><b>
What you will be doing
</b></p><ul><li>Conducting site qualification, initiation, monitoring, and close-out visits for clinical trials.</li><li>
Ensuring protocol compliance, data integrity, and patient safety throughout the trial process.</li><li>
Collaborating with investigators and site staff to facilitate smooth study conduct.</li><li>
Performing data review and resolution of queries to maintain high-quality clinical data.</li><li>
Contributing to the preparation and review of study documentation, including protocols and clinical study reports</li></ul><p><b><br>
Your profile
</b></p><ul><li>Bachelor's degree in a scientific or healthcare-related field.</li><li>
Minimum of 2 years of experience as a Clinical Research Associate.</li><li>
In-depth knowledge of clinical trial processes, regulations, and ICH-GCP guidelines.</li><li>
Strong organizational and communication skills, with attention to detail.</li><li>
Ability to work independently and collaboratively in a fast-paced environment.</li><li>
Experience in ophthalmology or gene therapy studies</li><li>
Ability to travel at least 60% of the time (international and domestic - fly and drive) and should possess a valid driver&rsquo;s license</li></ul><p></p><p><b>
What ICON can offer you:</b></p><p></p><div><div><div><div><p>
Our success depends on the quality of our people. That&rsquo;s why we&rsquo;ve made it a priority to build a diverse culture that rewards high performance and nurtures talent.</p><p></p><p>
In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family.</p><p></p><p>
Our benefits examples include:</p><ul><li><p>
Various annual leave entitlements</p></li><li><p>
A range of health insurance offerings to suit you and your family&rsquo;s needs.</p></li><li><p>
Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead.</p></li><li><p>
Global Employee Assistance Programme, TELUS Health, offering 24-hour access to a global network of over 80,000 independent specialised professionals who are there to support you and your family&rsquo;s well-being.</p></li><li><p>
Life assurance</p></li><li><p>
Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidised travel passes, health assessments, among others.</p></li></ul></div></div></div></div><p></p><p>
Visit our careers site to read more about the benefits ICON offers.</p><p></p><p>
At ICON, inclusion &amp; belonging are fundamental to our culture and values. We&rsquo;re dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.</p><p></p><div><div><div><div><p>
If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know</p><p></p><div><p>
Interested in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless &ndash; there&rsquo;s every chance you&rsquo;re exactly what we&rsquo;re looking for here at ICON whether it is for this or other roles.</p></div></div></div></div></div><p></p><p>
Salary Range</p>
$91,336.00-$114,170.00<p></p><p>
Bonus, Com, Stock, Benefits &amp; Disclaimer verbiage:</p><p>
Actual compensation will be determined based on factors such as geographic location, work experience, education/training, and skill level. You may be eligible for a bonus, stock compensation and commissions in some cases depending on your role and performance.</p></div><p></p>

Clinical Research Associate

RTI LABORATORIES

<p><b>Job Summary</b>  <br/>We are seeking a dynamic and detail-oriented Clinical Research Associate (CRA) to join our innovative clinical development team. In this vital role, you will oversee the planning, execution, and monitoring of clinical trials to ensure compliance with regulatory standards and study protocols. Your expertise will drive the successful management of clinical research projects, ensuring data integrity, patient safety, and adherence to all applicable regulations. This position offers an exciting opportunity to contribute to groundbreaking medical advancements while working in a collaborative and fast-paced environment.</p><p><b>Responsibilities</b></p><ul><li>Coordinate and monitor clinical trials across multiple sites, ensuring adherence to study protocols, FDA regulations, ICH GCP guidelines, and company standards.  </li><li>Conduct site qualification visits, initiate visits, routine monitoring visits, and close-out visits to verify compliance and data accuracy.  </li><li>Review and verify source documents, case report forms (CRFs), and other trial documentation for completeness and accuracy.  </li><li>Provide training and support to site staff on protocol procedures, data collection methods, EMR systems, and regulatory requirements.  </li><li>Monitor patient safety by reviewing adverse event reports, ensuring proper documentation, and reporting to relevant authorities as required.  </li><li>Manage trial documentation including ethics submissions, informed consent forms, regulatory binders, and audit readiness files.  </li><li>Collaborate with cross-functional teams such as clinical operations, data management, laboratory personnel, and medical staff to facilitate smooth trial execution.  </li><li>Ensure compliance with HIPAA regulations concerning patient confidentiality and data security.  </li><li>Assist in the review of clinical laboratory results, vital signs data, blood sampling procedures (phlebotomy), and other clinical assessments.  </li><li>Support statistical analysis activities by coordinating with statisticians using software tools designed for clinical data analysis.  </li><li>Maintain detailed records of site communications, monitoring reports, and trial progress for audit purposes.</li></ul><p><b>Experience</b></p><ul><li>Proven supervising experience in managing clinical trials or overseeing clinical research teams.  </li><li>Extensive knowledge of clinical trials management processes from initiation through close-out phases.  </li><li>Strong understanding of medical terminology, FDA regulations, ICH GCP guidelines, and CDISC standards for data exchange.  </li><li>Hands-on experience with EMR systems and electronic data capture (EDC) platforms for efficient data management.  </li><li>Background in nursing or clinical laboratory work (including blood sampling and vital signs measurement) is highly desirable.  </li><li>Familiarity with statistical software used in clinical research for data analysis purposes.  </li><li>Certification such as ICH GCP certificate from a recognized issuer (including CA) is required; additional certifications in HIPAA compliance or phlebotomy are a plus.  </li><li>Excellent analysis skills combined with meticulous attention to detail to ensure high-quality documentation review and compliance management. Join us in advancing medical science through rigorous research practices! We value energetic professionals committed to excellence in clinical development who thrive in collaborative environments dedicated to improving patient outcomes worldwide.</li></ul><p>Pay: $51,498.23 - $62,019.38 per year</p><p>Work Location: In person</p>

<div>Clinical Research Associate - California<p></p><p>
ICON plc is a world-leading healthcare intelligence and clinical research organization. We&rsquo;re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development</p><p></p><p>
As a CRA at ICON Plc, you will oversee and manage clinical trial activities to ensure they are conducted according to protocol, regulatory requirements, and industry standards.</p><p></p><p><b>
What You Will Do:</b></p><p></p><p>
You will lead on clinical trial monitoring tasks requiring technical depth, with a focus on quality and continuous improvement.<br>
<br>
Key responsibilities include:</p><ul><li><p>
Monitoring clinical trial sites to ensure adherence to study protocols, regulatory requirements, and Good Clinical Practice (GCP) standards.</p></li><li><p>
Conducting site visits to assess site performance, resolve issues, and provide support to ensure successful trial execution.</p></li><li><p>
Collaborating with cross-functional teams to ensure timely and accurate data collection and reporting.</p></li><li><p>
Providing training and guidance to site staff and other CRAs to maintain high standards of clinical trial conduct.</p></li><li><p>
Building and maintaining effective relationships with site personnel and stakeholders to facilitate smooth trial operations.</p></li></ul><p></p><p><b>
Your Profile:</b></p><p></p><p>
You will have a strong foundation in clinical trial monitoring, with the experience to work independently and guide others.<br>
<br>
Required qualifications and experience:</p><ul><li><p>
Bachelor's degree in a relevant scientific discipline or healthcare-related field</p></li><li><p>
Extensive experience as a Clinical Research Associate, with a strong understanding of clinical trial processes and regulatory requirements.</p></li><li><p>
Proven ability to manage multiple sites and projects simultaneously, with strong organizational and problem-solving skills.</p></li><li><p>
Expertise in monitoring practices, data integrity, and site management, with proficiency in relevant clinical trial software and tools.</p></li><li><p>
Excellent communication, interpersonal, and stakeholder management skills, with the ability to influence and drive compliance within a complex environment.</p></li><li><p>
Willingness to travel as required (approximately 60%)</p></li></ul><p></p><p><b>
What ICON can offer you:</b></p><p></p><div><div><div><div><p>
Our success depends on the quality of our people. That&rsquo;s why we&rsquo;ve made it a priority to build a diverse culture that rewards high performance and nurtures talent.</p><p></p><p>
In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family.</p><p></p><p>
Our benefits examples include:</p><ul><li><p>
Various annual leave entitlements</p></li><li><p>
A range of health insurance offerings to suit you and your family&rsquo;s needs.</p></li><li><p>
Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead.</p></li><li><p>
Global Employee Assistance Programme, TELUS Health, offering 24-hour access to a global network of over 80,000 independent specialised professionals who are there to support you and your family&rsquo;s well-being.</p></li><li><p>
Life assurance</p></li><li><p>
Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidised travel passes, health assessments, among others.</p></li></ul></div></div></div></div><p></p><p>
Visit our careers site to read more about the benefits ICON offers.</p><p></p><p>
At ICON, inclusion &amp; belonging are fundamental to our culture and values. We&rsquo;re dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.</p><p></p><div><div><div><div><p>
If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know</p><p></p><div><p>
Interested in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless &ndash; there&rsquo;s every chance you&rsquo;re exactly what we&rsquo;re looking for here at ICON whether it is for this or other roles.</p></div></div></div></div></div></div><p></p>

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Clinical Research Associate

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